Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3141–3160 of 27,451 recalls
Recalled Item: PACEMAKER PACK Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Vascular Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bilateral Tubal Ligation Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.7-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paracentesis Thoracente Recalled by American Contract Systems, Inc. Due to...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cath Lab Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT301US Airvo 3 Respiratory Support Device with software version 1.2.0...
The Issue: Due to a software issue, affected devices that are set up with High Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shoulder Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.7 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cysto Recalled by American Contract Systems, Inc. Due to ACS identified that...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.4 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.